Author

Sarah E. Bell

Babraham InstituteORCID 0000-0002-3249-707XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Organism:mouse· 3 Assay:bulk RNA-seq· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

Martin TurneriD· 3 shared Michelle A. LintermaniD· 2 shared Alex J. WhaleiD· 1 shared Anna Śledzińska· 1 shared Callum Baird NattressiD· 1 shared Ching‐In LauiD· 1 shared Christopher J. TapeiD· 1 shared Cristóbal CostoyaiD· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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3 shared papersImmunology

Martin TurnerORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Expression and role of the RNA-binding protein, ZFP36L1, in mouse T follicular helper cell differentiation and function

Helena A Carslaw, Sam Woolliscroft, Emily M. Watson, Sarah E. Bell, Michelle A. Linterman, Martin Turner, Louise M. C. Webb

This study investigates ZFP36L1's role in Tfh cell differentiation and function, finding that its deletion does not impair GC response or affinity maturation.

European Journal of Immunology · Aug 1, 2026Peer-reviewedImmunology

RNA-binding proteins control the G2-M checkpoint of the germinal centre B cell

Fiamma Salerno, Alex J. Whale, Louise S. Matheson, Davide Maria Vespasiani, William S. Foster, Twm J. Mitchell, Michael Screen, Melanie Stammers, Sarah E. Bell, Daniel James Hodson, Hamish W. King, Michelle A. Linterman, Jonathan M. Houseley, Martin Turner

This study identifies ZFP36L1 and ZFP36L2 as RNA-binding proteins that regulate the G2-M checkpoint in GC B cells to prevent replication stress and maintain genome stability.

Science Immunology · Oct 31, 2025Peer-reviewedImmunology

A post-transcriptional regulatory checkpoint controls the response of tumor-infiltrating cytotoxic CD4+ T cells to immunotherapy

Maria Vila de Mucha, Julia Hlond, Cristóbal Costoya, Ching‐In Lau, Anna Śledzińska, Imran Uddin, Mariela Navarrete, Mansi Shah, Gerasimos Mastrokalos, Despoina Karagianni, Sarah E. Bell, Callum Baird Nattress, Gordon Beattie, Christopher J. Tape, Martin Turner, , Richard G. Jenner

The paper identifies a post-transcriptional regulatory checkpoint, ZFP36/ZFP36L1, that controls CD4+ T cell cytotoxicity and response to immunotherapy.

bioRxiv · Sep 9, 2025 · PreprintImmunology